Site-specific oxidation of angiotensin I by copper(II) and l-ascorbate: Conversion of histidine residues to 2-imidazolones
- 2 November 1990
- journal article
- research article
- Published by Elsevier in Archives of Biochemistry and Biophysics
- Vol. 283 (1) , 20-26
- https://doi.org/10.1016/0003-9861(90)90606-y
Abstract
No abstract availableThis publication has 34 references indexed in Scilit:
- Ascorbate-mediated specific modification of histidine-containing peptidesJournal of Agricultural and Food Chemistry, 1989
- Selective oxidation of imidazole ring in histidine residues by the ascorbic acid — copper ion systemBiochemical and Biophysical Research Communications, 1986
- On the cytotoxicity of vitamin C and metal ionsEuropean Journal of Biochemistry, 1983
- CLEAVAGE OF THE IMIDAZOLE RING IN HISTIDYL RESIDUE ANALOGUES REACTED WITH PEROXIDIZING LIPIDSJournal of Food Science, 1979
- A Research Note REACTION PRODUCTS OF HISTIDINE WITH AUTOXIDIZED METHYL LINOLEATEJournal of Food Science, 1973
- Sensitized photooxidation of histidine and its derivatives. Products and mechanism of the reactionBiochemistry, 1969
- Kinetics of metal ion and metal chelate catalyzed oxidation of ascorbic acid. III. Vanadyl ion catalyzed oxidationJournal of the American Chemical Society, 1968
- Metal ion and metal chelate catalyzed oxidation of ascorbic acid by molecular oxygen. II. Cupric and ferric chelate catalyzed oxidationJournal of the American Chemical Society, 1967
- Metal ion and metal chelate catalyzed oxidation of ascorbic acid by molecular oxygen. I. Cupric and ferric ion catalyzed oxidationJournal of the American Chemical Society, 1967
- Photolysis of L-HistidineNature, 1965